A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14343844



Internal ID22268918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5989262..5989558hg38UCSC Ensembl
chr9:5989262..5989558hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229180
Supporting Variants
SamplesNA19238
Known GenesKIAA2026
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14343844
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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